🔍 RecallPedia

BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)

Class I - Dangerous
🏥 Medical Devices Recalled: October 12, 2022 Becton Dickinson Infusion Therapy Systems Surgical Instruments

What Should You Do?

  1. Check if you have this product:
    Catalog Number: 383516 UDI-DI Code: (01)00382903835164 Lot Number: 2168865
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Becton Dickinson Infusion Therapy Systems Inc.
Reason for Recall:
During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)

Product Codes/Lot Numbers:

Catalog Number: 383516 UDI-DI Code: (01)00382903835164 Lot Number: 2168865

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0174-2023

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